EP1694718A1 - Membranes a electrolyte polymere reticulees par fluoration directe - Google Patents

Membranes a electrolyte polymere reticulees par fluoration directe

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Publication number
EP1694718A1
EP1694718A1 EP04811655A EP04811655A EP1694718A1 EP 1694718 A1 EP1694718 A1 EP 1694718A1 EP 04811655 A EP04811655 A EP 04811655A EP 04811655 A EP04811655 A EP 04811655A EP 1694718 A1 EP1694718 A1 EP 1694718A1
Authority
EP
European Patent Office
Prior art keywords
polymer
typically
groups
perfluorinated
crosslinked
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04811655A
Other languages
German (de)
English (en)
Inventor
Miguel A. Guerra
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
3M Innovative Properties Co
Original Assignee
3M Innovative Properties Co
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Filing date
Publication date
Application filed by 3M Innovative Properties Co filed Critical 3M Innovative Properties Co
Publication of EP1694718A1 publication Critical patent/EP1694718A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
    • C08F8/18—Introducing halogen atoms or halogen-containing groups
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/1058—Polymeric electrolyte materials characterised by a porous support having no ion-conducting properties
    • H01M8/106—Polymeric electrolyte materials characterised by a porous support having no ion-conducting properties characterised by the chemical composition of the porous support
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
    • C08F8/18—Introducing halogen atoms or halogen-containing groups
    • C08F8/20—Halogenation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00—Processes of treating or compounding macromolecular substances
    • C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/20—Manufacture of shaped structures of ion-exchange resins
    • C08J5/22—Films, membranes or diaphragms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/20—Manufacture of shaped structures of ion-exchange resins
    • C08J5/22—Films, membranes or diaphragms
    • C08J5/2206—Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
    • C08J5/2218—Synthetic macromolecular compounds
    • C08J5/2231—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds
    • C08J5/2237—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds containing fluorine
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/20—Manufacture of shaped structures of ion-exchange resins
    • C08J5/22—Films, membranes or diaphragms
    • C08J5/2206—Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
    • C08J5/2275—Heterogeneous membranes
    • C08J5/2281—Heterogeneous membranes fluorine containing heterogeneous membranes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/102—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer
    • H01M8/1023—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer having only carbon, e.g. polyarylenes, polystyrenes or polybutadiene-styrenes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/1039—Polymeric electrolyte materials halogenated, e.g. sulfonated polyvinylidene fluorides
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/1069—Polymeric electrolyte materials characterised by the manufacturing processes
    • H01M8/1072—Polymeric electrolyte materials characterised by the manufacturing processes by chemical reactions, e.g. insitu polymerisation or insitu crosslinking
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/1069—Polymeric electrolyte materials characterised by the manufacturing processes
    • H01M8/1086—After-treatment of the membrane other than by polymerisation
    • H01M8/1088—Chemical modification, e.g. sulfonation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
    • C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2327/12—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C08J2327/18—Homopolymers or copolymers of tetrafluoroethylene
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0065—Solid electrolytes
    • H01M2300/0082—Organic polymers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/50—Fuel cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the invention relates to a crosslinked polymer electrolyte membrane made by a method that comprises the step of direct fluorination of a non-perfluorinated polymer, typically highly fluorinated polymer, comprising first pendent groups which comprise sulfonyl halide groups, or direct fluorination of a polymer mixture of a first polymer which is a non-perfluorinated polymer and a second polymer which comprises first pendent groups which comprise sulfonyl halide groups.
  • the process may be used to make crosslinked polymer electrolyte membranes (PEM's) which may be used in electrolytic cells such as fuel cells.
  • PEM's crosslinked polymer electrolyte membranes
  • Nafion® by DuPont Chemical Company, Wilmington, Delaware. Nafion® is commonly used in making polymer electrolyte membranes for use in fuel cells.
  • Copolymers of tetrafluoroethylene (TFE) and a co-monomer according to the formula: FSO2-CF2-CF2-OOF IF2 are known and used in sulfonic acid form, i.e., with the FSO2- end group hydrolyzed to HSO3-, in making polymer electrolyte membranes for use in fuel cells.
  • a polymer electrolyte membrane having a thickness of 90 microns or less and comprising a polymer, said polymer comprising a highly fluorinated backbone and recurring pendant groups according to the formula: YOSO 2 -CF2-CF2-CF 2 -CF2-O-[ ⁇ olymer backbone] where Y is H + or a monovalent cation such as an alkali metal cation.
  • the membrane is a cast membrane.
  • the polymer has a hydration product of greater than 22,000.
  • the polymer has an equivalent weight of 800-1200.
  • 6,277,512 discloses a polymer electrolyte membrane comprising an intimate mixture of an ionomeric polymer and a structural film-forming polymer. Optionally, one or both are crosslinked.
  • U.S. Patent No. 5,986,012 purportedly discloses a process for fluorinating a perfluoroelastomer which has previously been crosslinked by exposure to ionizing radiation, which purportedly results in a product with reduced outgassing.
  • U.S. Patent No. 4,755,567 purportedly discloses a process for direct fluorination of ethers in the presence of hydrogen fluoride scavengers such as sodium fluoride and potassium fluoride.
  • [F]luorocarbon polymers can be produced with chemical compositions very similar to polytetrafluoroethylene by the direct reaction of fluorine with polyethylene and the perfluoroanalogues of polypropylene and polystyrene can be prepared. These fluorocarbon polymers differ from the more familiar linear structures because carbon- carbon cross-linking occurs to a significant extent during fluorination.”
  • the present invention provides a method of making a crosslinked polymer comprising the steps of: a) providing a non-perfluorinated polymer comprising first pendent groups which comprise sulfonyl halide groups; and b) direct fluorinating the polymer.
  • the method may additionally comprise, prior to step b) of direct fluorinating the polymer, the step of: c) forming said polymer into a membrane, typically having a thickness of 90 microns or less, more typically 60 microns or less, and most typically 30 microns or less.
  • the method may additionally comprise, after step b) of direct fluorinating the polymer, the step of: d) converting the sulfonyl halide groups to sulfonic acid groups.
  • the non-perfluorinated polymer may be highly fluorinated.
  • the non-perfluorinated polymer may be a polymer of monomers which include tetrafluoroethylene (TFE) and vinylidene fluoride (VDF).
  • the first pendent groups may be according to the formula: -R.I-SO2X, where X is a halogen and where R* is a branched or unbranched perfluoroalkyl or perfluoroether group comprising 1-15 carbon atoms and 0-4 oxygen atoms, such as -O-CF2-CF2-CF2-CF2-SO2X or -O-CF 2 -
  • step c) may comprise imbibing the polymer into a porous supporting matrix, such as a porous polytetrafluoroethylene web or a porous web of a highly fluorinated, non-perfluorinated polymer.
  • a porous supporting matrix such as a porous polytetrafluoroethylene web or a porous web of a highly fluorinated, non-perfluorinated polymer.
  • the present invention provides a method of making a crosslinked polymer comprising the steps of: a) providing a polymer mixture of a first polymer which is a non-perfluorinated polymer and a second polymer which comprises first pendent groups which comprise sulfonyl halide groups; and b) direct fluorinating the polymer mixture.
  • the method may additionally comprise, prior to step b) of direct fluorinating the polymer mixture, the step of: c) forming said polymer into a membrane, typically having a thickness of 90 microns or less, more typically 60 microns or less, and most typically 30 microns or less.
  • the method may additionally comprise, after step b) of direct fluorinating the polymer mixture, the step of: d) converting the sulfonyl halide groups to sulfonic acid groups.
  • the first polymer may be a copolymer of tetrafluoroethylene (TFE) and vinylidene fluoride (VDF).
  • the first polymer may be a terpolymer of tetrafluoroethylene (TFE), hexafluoropropylene (HFP) and vinylidene fluoride (VDF).
  • the second polymer may be perfluorinated or non-perfluorinated.
  • the first pendent groups may be according to the formula:
  • step c) may comprise imbibing the polymer mixture into a porous supporting matrix, such as a porous polytetrafluoroethylene web or a porous web of a highly fluorinated, non-perfluorinated polymer.
  • the present invention provides polymer electrolyte membranes comprising the crosslinked polymers made according to any of the methods of the present invention.
  • the present invention provides polymer electrolyte membranes made according to any of the methods of the present invention.
  • equivalent weight E W
  • HP hydrolysis product
  • high highly fluorinated means containing fluorine in an amount of 40 wt% or more, typically 50 wt% or more and more typically 60 wt% or more.
  • the present invention provides a crosslinked polymer, typically a polymer electrolyte membrane, made by direct fluorination of a non-perfluorinated polymer comprising first pendent groups which comprise sulfonyl halide groups or by direct fluorination of a polymer mixture of a first polymer which is a non-perfluorinated polymer and a second polymer which comprises first pendent groups which comprise sulfonyl halide groups.
  • Such crosslinked polymers or polymer mixtures may be used to make polymer electrolyte membranes (PEM's) that may be used in electrolytic cells such as fuel cells.
  • PEM's manufactured from the crosslinked polymer according to the present invention may be used in the fabrication of membrane electrode assemblies (MEA's) for use in fuel cells.
  • An MEA is the central element of a proton exchange membrane fuel cell, such as a hydrogen fuel cell.
  • Fuel cells are electrochemical cells which produce usable electricity by the catalyzed combination of a fuel such as hydrogen and an oxidant such as oxygen.
  • Typical MEA's comprise a polymer electrolyte membrane (PEM) (also known as an ion conductive membrane (ICM)), which functions as a solid electrolyte.
  • PEM polymer electrolyte membrane
  • ICM ion conductive membrane
  • GDL Gas diffusion layer layers
  • FTL fluid transport layer
  • DCC diffuser/current collector
  • the anode and cathode electrode layers may be applied to opposite sides of the PEM in the fonn of a catalyst ink, and the resulting catalyst-coated membrane (CCM) sandwiched with two GDL's to form a five-layer MEA.
  • the five layers of a five-layer MEA are, in order: anode GDL, anode electrode layer, PEM, cathode electrode layer, and cathode GDL.
  • protons are formed at the anode via hydrogen oxidation and transported across the PEM to the cathode to react with oxygen, causing electrical current to flow in an external circuit connecting the electrodes.
  • a non-perfluorinated polymer comprising first pendent groups which comprise sulfonyl halide groups is direct fluorinated.
  • the polymer having first pendent groups must be non-perfluorinated in this first embodiment.
  • a polymer mixture of a first polymer which is a non-perfluorinated polymer and a second polymer which comprises first pendent groups which comprise sulfonyl halide groups is direct fluorinated.
  • the polymer having first pendent groups may be perfluorinated or non- perfluorinated in this second embodiment.
  • the first polymer must be non- perfluorinated in this second embodiment.
  • the polymer having first pendent groups used in the method according to the present invention comprises a backbone, which may be branched or unbranched but is typically unbranched, and first pendent groups. Where this polymer is non- perfluorinated, hydrogens may appear in the backbone or in the side groups, but more typically appear in the backbone.
  • first side groups R may be added to the backbone by grafting.
  • first side groups R are highly fluorinated, having between 50% and 100% of hydrogens substituted with fluorine.
  • R is -RI-SO2X, where Rl is a branched or unbranched perfluoroalkyl or perfluoroether group comprising 1-15 carbon atoms and
  • Rl is typically -O-R ⁇ - wherein R2 is a branched or unbranched perfluoroalkyl or perfluoroether group comprising 1-15 carbon atoms and 0-4 oxygen atoms.
  • R ⁇ is more typically -O-R3- wherein R3 is a perfluoroalkyl group comprising 1-15 carbon atoms.
  • Rl examples include: -(CF 2 ) n - where n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15 (-CF 2 CF(CF 3 )-) n where n is 1, 2, 3, 4, or 5 (-CF(CF 3 )CF 2 -) n where n is 1, 2, 3, 4, or 5(-CF 2 CF(CF 3 )-) n -CF 2 - where n is 1, 2, 3 or 4 (-O-CF2CF2-) n where n is 1 , 2, 3, 4, 5, 6 or 7 (-O-CF2CF2CF2-) n where n is 1, 2, 3, 4, or 5 (-O-CF2CF2CF2CF2-) n where n is 1, 2 or 3 (-O-CF2CF(CF3)-) n where n is 1, 2, 3, 4, or 5 (-O-CF 2 CF(CF 3 )CF 2 -) n where n is 1, 2 or 3 (-O-CF(CF 3 )CF 2 -)
  • the -SO2X group is most typically -SO2F during polymerization, i.e., X is F, and the sulfonyl fluoride group is typically hydrolyzed to -SO3H prior to use of the fluoropolymer as an ionomer.
  • Fluoromonomers providing first side group R may be synthesized by any suitable means, including methods disclosed in U.S. Pat. No. 6,624,328.
  • the first polymer may be any suitable non-perfluorinated polymer, including copolymers of tetrafluoroethylene (TFE) and vinylidene fluoride (VDF) and terpolymers of tetrafluoroethylene (TFE), hexafluoropropylene (HFP) and vinylidene fluoride (VDF), which may be known as THV polymers.
  • a non-fluorinated polymer may be used, such as polyethylene, polypropylene, and the like. Fluorine and hydrogen content of the first polymer are typically determined so as to provide adequate crosslinking and adequate miscibility with the second polymer.
  • the polymers may be made by any suitable method, including emulsion polymerization, extrusion polymerization, polymerization in supercritical carbon dioxide, solution or suspension polymerization, and the like, which may be batchwise or continuous.
  • First and second polymers may be mixed by any suitable method, including mixing in solution or suspension, kneading, milling, or the like.
  • the ratio of first and second polymers is typically determined so as to provide adequate crosslinking and satisfy the hydration product and equivalent weight terms described below.
  • the mixture contains 1-50%, more typically 1-25%, and more typically 1-10% of the first polymer. Where less fluorinated or unfluorinated first polymers are used, it may be possible to use smaller amounts of the first polymer and achieve the desired degree of crosslinking.
  • the polymer or polymer mixture is formed into a membrane prior to crosslinking.
  • Any suitable method of forming the membrane may be used.
  • the polymer or polymer mixture is typically cast from a suspension or solution. Any suitable casting method may be used, including bar coating, spray coating, slit coating, brush coating, and the like.
  • the membrane may be formed from neat polymer or polymer mixture in a melt process such as extrusion. After forming, the membrane may be annealed.
  • the membrane has a thickness of 90 microns or less, more typically 60 microns or less, and most typically 30 microns or less. A thinner membrane may provide less resistance to the passage of ions. In fuel cell use, this results in cooler operation and greater output of usable energy.
  • the polymer or polymer mixture may be imbibed into a porous supporting matrix prior to crosslinking, typically in the form of a thin membrane having a thickness of 90 microns or less, more typically 60 microns or less, and most typically 30 microns or less.
  • Any suitable method of imbibing the polymer or polymer mixture into the pores of the supporting matrix may be used, including overpressure, vacuum, wicking, immersion, and the like.
  • the polymer or polymer mixture becomes embedded in the matrix upon crosslinking.
  • Any suitable supporting matrix may be used. Typically the supporting matrix is electrically non-conductive.
  • the supporting matrix is composed of a fluoropolymer, which may be perfluorinated or more typically non-perfluorinated.
  • a fluoropolymer which may be perfluorinated or more typically non-perfluorinated.
  • the process of direct fluorination may covalently bind the matrix to the polymer or polymer mixture imbibed therein.
  • Typical perfluorinated matrices include porous polytetrafluoroethylene (PTFE), such as biaxially stretched PTFE webs.
  • Typical non- perfluorinated matrices include webs of TFE/VDF copolymers. Additional embodiments maybe found in U.S. Pats. Nos. RE37,307, RE37,656, RE37/701, and
  • the step of crosslinking is accomplished by direct fluorination, i.e., by application of fluorine gas to the polymer.
  • Any suitable process may be used, including the LaMar process or other processes described or cited in the references listed in the
  • the fluorine gas is diluted with nitrogen gas, the mixture typically containing 5-40% fluorine by volume.
  • Typical reaction temperatures are between -20 °C and 150 °C. Lower temperatures may prevent removal of sulfonyl halide groups from the polymer.
  • backbone and side-chain hydrogens may be abstracted in the fluorination process, leaving reactive radicals which form crosslinks.
  • Crosslinking may occur before or after annealing.
  • the resulting crosslinked polymer is typically perfluorinated or nearly perfluorinated.
  • the sulfur-containing functions of the first pendant groups may be converted to sulfonic acid form by any suitable process, such as hydrolysis.
  • the polymer is immersed in an aqueous solution of LiOH, NaOH or
  • the acid-functional pendent groups typically are present in the polymer or polymer mixture in an amount sufficient to result in an hydration product (HP) of greater than 22,000, more typically greater than 23,000, more typically greater than
  • the acid-functional pendent groups typically are present in the polymer or polymer mixture in an amount sufficient to result in an equivalent weight (EW) of less than 1200, more typically less than 1100, and more typically less than 1000, and more typically less than 900.
  • EW equivalent weight
  • membranes made according to the method of the present invention may differ in chemical structure from those made by other methods, in the structure of crosslinks, the placement of crosslinks, the placement of acid- functional groups, the presence or absence of crosslinks on pendent groups or of acid- functional groups on crosslinks, and the like.

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  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Sustainable Development (AREA)
  • Sustainable Energy (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Fuel Cell (AREA)
  • Conductive Materials (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

L'invention concerne un procédé destiné à fabriquer un polymère réticulé par la fluoration directe d'un polymère non perfluoré comprenant des premiers groupes latéraux qui comprennent des groupes d'halogénures de sulfonyle ou par la fluoration directe d'un mélange de polymères d'un premier polymère qui est un polymère non perfluoré et d'un deuxième polymère, qui comprend des premiers groupes latéraux qui contiennent des groupes d'halogénures de sulfonyle. Ces polymères ou ces mélanges de polymères réticulés peuvent s'utiliser pour fabriquer des membranes d'électrolytes polymères (des PEM) qui peuvent s'utiliser dans des cellules électrolytiques telles que les piles à combustible, et qui peuvent manifester une plus grande durabilité lors de l'usage des piles à combustible.
EP04811655A 2003-12-17 2004-11-19 Membranes a electrolyte polymere reticulees par fluoration directe Withdrawn EP1694718A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/738,083 US7173067B2 (en) 2003-12-17 2003-12-17 Polymer electrolyte membranes crosslinked by direct fluorination
PCT/US2004/038966 WO2005061559A1 (fr) 2003-12-17 2004-11-19 Membranes a electrolyte polymere reticulees par fluoration directe

Publications (1)

Publication Number Publication Date
EP1694718A1 true EP1694718A1 (fr) 2006-08-30

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP04811655A Withdrawn EP1694718A1 (fr) 2003-12-17 2004-11-19 Membranes a electrolyte polymere reticulees par fluoration directe

Country Status (8)

Country Link
US (2) US7173067B2 (fr)
EP (1) EP1694718A1 (fr)
JP (1) JP2007517095A (fr)
KR (1) KR20070008544A (fr)
CN (1) CN100560612C (fr)
CA (1) CA2550285A1 (fr)
TW (1) TW200533687A (fr)
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